The following data is part of a premarket notification filed by Levitronix Llc. with the FDA for Levitronix Centrimag Back-up Console.
| Device ID | K051209 |
| 510k Number | K051209 |
| Device Name: | LEVITRONIX CENTRIMAG BACK-UP CONSOLE |
| Classification | Pump, Blood, Cardiopulmonary Bypass, Non-roller Type |
| Applicant | LEVITRONIX LLC. 45 FIRST AVE. Waltham, MA 02451 |
| Contact | Farzad Parsaie |
| Correspondent | Farzad Parsaie LEVITRONIX LLC. 45 FIRST AVE. Waltham, MA 02451 |
| Product Code | KFM |
| CFR Regulation Number | 870.4360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-05-11 |
| Decision Date | 2005-09-08 |
| Summary: | summary |